Zodryl Ac 80
Product Images NDC 43378-106

3 FDA label images from Codadose, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Zodryl Ac 80 (NDC 43378-106). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Codadose, Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

1600c314-figure-01 (1600c314 Figure 01)

1600c314-figure-01 (1600c314 Figure 01)
The packaging label for Zodryl AC 80 by CodaDose, Inc. shows an 8 fl oz (236 mL) liquid dosage form with grape flavor. The label highlights active ingredients Chlorpheniramine maleate (antihistamine) and Codeine phosphate (cough suppressant). It includes warnings, NDC 43378-106-08, and dosage instructions referencing the codeDOSE oral dispenser.*
FDA Label Image

1600c314-figure-02 (1600c314 Figure 02)

1600c314-figure-02 (1600c314 Figure 02)
Packaging label for Zodryl AC 80 by CodaDose, Inc. The label displays Drug Facts panels including active ingredients and purposes, as well as usage directions. The label also includes a barcode and measurements for folding. It is intended for a product with NDC 43378-106.*
FDA Label Image

1600c314-figure-03 (1600c314 Figure 03)

1600c314-figure-03 (1600c314 Figure 03)
This image shows the back cover panels of Drug Facts information with dimensions for two pages, labeled as Page #2 and Page #3. The panels include drug warnings, directions, usage information, and other drug facts text typically found on medication packaging. The text is structured in sections with headings for clear readability.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.